SNP Report

Basic Info

Name	rs12304817 dbSNP Ensembl
Location	chr12:102219760 - 102219760(1)
Variant Alleles	C/G
Ancestral Allele	G
Minor Allele	G
Minor Allele Frequence	0.388578
Functional Annotation	non_coding_transcript_exon_variant; non_coding_transcript_variant; upstream_gene_variant.
Consequence to Transcript	non_coding_transcript_exon_variant(ENST00000626826); non_coding_transcript_variant(ENST00000626826); upstream_gene_variant(ENST00000583259)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
RN7SL793P	RNA, 7SL, cytoplasmic 793, pseudogene	12q23.2	Mapped by LD-proxy

SNPs in LD with rs12304817 (count: 0) View in gBrowse (chr12:102219760..102219760 )

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)